Molecular cloning and characterization of a cDNA encoding mouse phospholipase C-β31

Shu Wang , Yinghua Zhou , Agneta Lukinius , Kjell Öberg , Britt Skogseid , Anders Gobl
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引用次数: 5

Abstract

A cDNA encoding mouse PLC-β3 (mPLC-β3) was identified by screening a mouse kidney cDNA library and using the rapid amplification of cDNA ends (RACE) method. The predicted open reading frame was 3705 bp in length. The deduced 1235 amino acid (aa) sequence shares 95.3% and 92% homology with the sequences of rat and human PLC-β3, respectively. The corresponding mRNA is highly expressed in kidney, skeletal muscle, liver, lung, heart and brain. In spleen, mPLC-β3 mRNA was not detectable, which is in contrast to humans where there is a distinct expression. Using ultrastructural immunocytochemistry, mPLC-β3 expression was detected in the heterochromatin of the nucleus in mouse brain neurons. The observation of PLC-β3 nuclear localization suggests that PLC-β3 may have intranuclear functions.

小鼠磷脂酶C-β31 cDNA的克隆及特性分析
通过筛选小鼠肾脏cDNA文库,采用cDNA末端快速扩增(RACE)方法,鉴定了一段编码小鼠PLC-β3的cDNA (mPLC-β3)。预测的开放阅读框长度为3705 bp。所得1235个氨基酸(aa)序列与大鼠和人PLC-β3序列同源性分别为95.3%和92%。相应的mRNA在肾脏、骨骼肌、肝脏、肺、心脏和大脑中高表达。在脾脏中,未检测到mPLC-β 3mrna,这与人类有明显表达的情况相反。应用超微结构免疫细胞化学方法,检测了mPLC-β3在小鼠脑神经细胞细胞核异染色质中的表达。对PLC-β3核定位的观察表明,PLC-β3可能具有核内功能。
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